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WO2009071680A3 - Composés d'antagonistes d'arn utiles pour moduler mcl-1 - Google Patents

Composés d'antagonistes d'arn utiles pour moduler mcl-1 Download PDF

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Publication number
WO2009071680A3
WO2009071680A3 PCT/EP2008/066920 EP2008066920W WO2009071680A3 WO 2009071680 A3 WO2009071680 A3 WO 2009071680A3 EP 2008066920 W EP2008066920 W EP 2008066920W WO 2009071680 A3 WO2009071680 A3 WO 2009071680A3
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WIPO (PCT)
Prior art keywords
mcl
modulation
expression
antagonist compounds
oligonucleotides
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2008/066920
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English (en)
Other versions
WO2009071680A2 (fr
Inventor
Jens Bo Hansen
Anja Moelhart Hoeg
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Roche Innovation Center Copenhagen AS
Original Assignee
Santaris Pharma AS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Santaris Pharma AS filed Critical Santaris Pharma AS
Priority to US12/746,745 priority Critical patent/US20100323967A1/en
Priority to JP2010536479A priority patent/JP2011505798A/ja
Priority to EP08855783A priority patent/EP2238249A2/fr
Publication of WO2009071680A2 publication Critical patent/WO2009071680A2/fr
Publication of WO2009071680A3 publication Critical patent/WO2009071680A3/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • CCHEMISTRY; METALLURGY
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    • C12N15/00Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
    • C12N15/09Recombinant DNA-technology
    • C12N15/11DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
    • C12N15/113Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • C12N15/1135Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against oncogenes or tumor suppressor genes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/10Type of nucleic acid
    • C12N2310/11Antisense
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    • C12N2310/00Structure or type of the nucleic acid
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    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/30Chemical structure
    • C12N2310/32Chemical structure of the sugar
    • C12N2310/3212'-O-R Modification
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    • C12N2310/00Structure or type of the nucleic acid
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    • C12N2310/30Chemical structure
    • C12N2310/32Chemical structure of the sugar
    • C12N2310/323Chemical structure of the sugar modified ring structure
    • C12N2310/3231Chemical structure of the sugar modified ring structure having an additional ring, e.g. LNA, ENA
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    • C12N2310/34Spatial arrangement of the modifications
    • C12N2310/341Gapmers, i.e. of the type ===---===
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    • C12N2310/00Structure or type of the nucleic acid
    • C12N2310/30Chemical structure
    • C12N2310/34Spatial arrangement of the modifications
    • C12N2310/346Spatial arrangement of the modifications having a combination of backbone and sugar modifications

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  • Health & Medical Sciences (AREA)
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  • Child & Adolescent Psychology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

On a mis au point des oligonucléotides dirigés contre le gène Mcl-1 afin de moduler l'expression de la protéine Mcl-1. Les compositions comprennent des oligonucléotides, notamment des oligonucléotides antisens, ciblés sur des acides nucléiques codant Mcl-1. Cette invention porte également sur des méthodes d'utilisation de ces composés en vue de moduler l'expression de Mcl-1 et pour le traitement de maladies associées à la surexpression de Mcl-1. Des exemples de ces maladies sont le cancer et la mastocytose généralisée.
PCT/EP2008/066920 2007-12-07 2008-12-05 Composés d'antagonistes d'arn utiles pour moduler mcl-1 Ceased WO2009071680A2 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
US12/746,745 US20100323967A1 (en) 2007-12-07 2008-12-05 RNA Antagonist Compounds for the Modulation of MCL-1
JP2010536479A JP2011505798A (ja) 2007-12-07 2008-12-05 Mcl−1を調節するためのRNAアンタゴニスト化合物
EP08855783A EP2238249A2 (fr) 2007-12-07 2008-12-05 Composés d'antagonistes d'arn utiles pour moduler mcl-1

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US1219107P 2007-12-07 2007-12-07
US61/012,191 2007-12-07
US9595508P 2008-09-11 2008-09-11
US61/095,955 2008-09-11

Publications (2)

Publication Number Publication Date
WO2009071680A2 WO2009071680A2 (fr) 2009-06-11
WO2009071680A3 true WO2009071680A3 (fr) 2009-07-23

Family

ID=40329152

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2008/066920 Ceased WO2009071680A2 (fr) 2007-12-07 2008-12-05 Composés d'antagonistes d'arn utiles pour moduler mcl-1

Country Status (4)

Country Link
US (1) US20100323967A1 (fr)
EP (1) EP2238249A2 (fr)
JP (1) JP2011505798A (fr)
WO (1) WO2009071680A2 (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2907694A1 (fr) * 2013-05-24 2014-11-27 Roche Innovation Center Copenhagen A/S Modulateurs oligonucleotidiques de la leucemie lymphocytaire chronique a cellules b/lymphome 11a (bcl11a) et utilisations de ceux.ci
WO2017184082A1 (fr) * 2016-04-22 2017-10-26 Nanyang Technological University Oligonucléotide chimère de perméation de lymphocytes, procédés et utilisations associés
US11065230B2 (en) 2016-09-16 2021-07-20 Inserm (Institut National De La Sante Et De La Recherche Medicale) Methods and pharmaceutical compositions for the treatment of systemic mastocytosis
WO2018181428A1 (fr) 2017-03-29 2018-10-04 塩野義製薬株式会社 Complexe de médicament d'acide nucléique et de lipide multiramifié
EP4005602A4 (fr) 2019-07-30 2024-06-12 Shionogi & Co., Ltd Médicament à base d'acide nucléique ciblant le murf1
JP7751302B2 (ja) 2020-06-15 2025-10-08 リードファーマ株式会社 架橋型ヌクレオシドおよびヌクレオチド

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001511000A (ja) * 1997-01-31 2001-08-07 バイオグノスティック ゲゼルシャフト フュア バイオモレキュラー ダイアグノスティック ミット ベシュレンクテル ハフツング アンチセンスオリゴヌクレオチドの製造方法
WO2004048511A2 (fr) * 2002-11-26 2004-06-10 Rosetta Genomics Ltd. Groupe detectable par bio-informatique, de nouveaux genes regulateurs viraux, et utilisations de ceux-ci
WO2007109174A2 (fr) * 2006-03-16 2007-09-27 Isis Pharmaceuticals, Inc. Compositions et procedes de modulation de l'expression de mcl-1

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9711919D0 (en) * 1997-06-09 1997-08-06 Ciba Geigy Ag Oligonucleotide derivatives
WO2007136989A2 (fr) * 2006-05-05 2007-11-29 Isis Pharmaceuticals, Inc. Composés et procédés pour moduler l'expression de dgat2

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2001511000A (ja) * 1997-01-31 2001-08-07 バイオグノスティック ゲゼルシャフト フュア バイオモレキュラー ダイアグノスティック ミット ベシュレンクテル ハフツング アンチセンスオリゴヌクレオチドの製造方法
WO2004048511A2 (fr) * 2002-11-26 2004-06-10 Rosetta Genomics Ltd. Groupe detectable par bio-informatique, de nouveaux genes regulateurs viraux, et utilisations de ceux-ci
WO2007109174A2 (fr) * 2006-03-16 2007-09-27 Isis Pharmaceuticals, Inc. Compositions et procedes de modulation de l'expression de mcl-1

Non-Patent Citations (11)

* Cited by examiner, † Cited by third party
Title
AICHBERGER K J ET AL: "Identification of MCL1 as a novel target in neoplastic mast cells in systemic mastocytosis: Inhibition of mast cell survival by MCL1 antisense oligonucleotides and synergism with PKC412", BLOOD, AMERICAN SOCIETY OF HEMATOLOGY, US, vol. 109, no. 7, 1 April 2007 (2007-04-01), pages 3031 - 3041, XP002478480, ISSN: 0006-4971 *
DATABASE EMBL [online] 14 December 2007 (2007-12-14), "Sequence 137 from Patent WO2007109174.", XP002514972, retrieved from EBI accession no. EMBL:CS811835 Database accession no. CS811835 *
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DATABASE EMBL [online] 29 December 2008 (2008-12-29), "SINGLE-STRANDED ANTIMICROBIAL OLIGONUCLEOTIDES AND USES THEREOF.", XP002514974, retrieved from EBI accession no. EMBL:DL465760 Database accession no. DL465760 *
DATABASE EMBL [online] 4 September 2002 (2002-09-04), "An antisense oligonucleotide preparation method.", XP002514976, retrieved from EBI accession no. EMBL:BD065789 Database accession no. BD065789 *
DATABASE Geneseq [online] 16 January 2002 (2002-01-16), "Validation ribozyme DNA sequence #92.", XP002514977, retrieved from EBI accession no. GSN:AAS56918 Database accession no. AAS56918 *
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JANSEN B ET AL: "Antisense therapy for cancer-the time of truth", LANCET ONCOLOGY, LANCET PUBLISHING GROUP, LONDON, GB, vol. 3, no. 11, 1 November 2002 (2002-11-01), pages 672 - 683, XP004810743, ISSN: 1470-2045 *
MOTT J L ET AL: "mir-29 regulates Mcl-1 protein expression and apoptosis", ONCOGENE, NATURE PUBLISHING GROUP, GB BASINGSTOKE, HANTS, vol. 26, no. 42, 12 April 2007 (2007-04-12), pages 6133 - 6140, XP002499484, ISSN: 0950-9232, [retrieved on 20070402] *
THALLINGER CHRISTIANE ET AL: "Mcl-1 antisense therapy chemosensitizes human melanoma in a SCID mouse xenotransplantation model.", THE JOURNAL OF INVESTIGATIVE DERMATOLOGY JUN 2003, vol. 120, no. 6, June 2003 (2003-06-01), pages 1081 - 1086, XP002515069, ISSN: 0022-202X *
WACHECK VOLKER ET AL: "Mcl-1 is a relevant molecular target for antisense oligonucleotide strategies in gastric cancer cells", CANCER BIOLOGY AND THERAPY, LANDES BIOSCIENCE, US, vol. 5, no. 10, 1 October 2006 (2006-10-01), pages 1348 - 1354, XP008084402, ISSN: 1538-4047 *

Also Published As

Publication number Publication date
US20100323967A1 (en) 2010-12-23
JP2011505798A (ja) 2011-03-03
EP2238249A2 (fr) 2010-10-13
WO2009071680A2 (fr) 2009-06-11

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